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Polarization analysis for small-angle neutron scattering with a $$^{3}$$He spin filter at a pulsed neutron source

奥平 琢也; 上田 祐生; 廣井 孝介; 元川 竜平; 稲村 泰弘; 高田 慎一; 奥 隆之; 鈴木 淳市*; 高橋 慎吾*; 遠藤 仁*; et al.

Journal of Applied Crystallography, 54(2), p.548 - 556, 2021/04

 被引用回数:0 パーセンタイル:0.02(Chemistry, Multidisciplinary)



Development and application of a $$^3$$He neutron spin filter at J-PARC

奥平 琢也; 奥 隆之; 猪野 隆*; 林田 洋寿*; 吉良 弘*; 酒井 健二; 廣井 孝介; 高橋 慎吾*; 相澤 一也; 遠藤 仁*; et al.

Nuclear Instruments and Methods in Physics Research A, 977, p.164301_1 - 164301_8, 2020/10

 被引用回数:3 パーセンタイル:78.97(Instruments & Instrumentation)

We are developing a neutron polarizer with polarized $$^3$$He gas, referred to as a $$^3$$He spin filter, based on the Spin Exchange Optical Pumping (SEOP) for polarized neutron scattering experiments at Materials and Life Science Experimental Facility (MLF) of Japan Proton Accelerator Research Complex (J-PARC). A $$^3$$He gas-filling station was constructed at J-PARC, and several $$^3$$He cells with long spin relaxation times have been fabricated using the gas-filling station. A laboratory has been prepared in the MLF beam hall for polarizing $$^3$$He cells, and compact pumping systems with laser powers of 30 W and 110 W, which can be installed onto a neutron beamline, have been developed. A $$^3$$He polarization of 85% was achieved at a neutron beamline by using the pumping system with the 110 W laser. Recently, the first user experiment utilizing the $$^3$$He spin filter was conducted, and there have been several more since then. The development and utilization of $$^3$$He spin filters at MLF of J-PARC are reported.


Status of neutron spectrometers at J-PARC

梶本 亮一; 横尾 哲也*; 中村 充孝; 川北 至信; 松浦 直人*; 遠藤 仁*; 瀬戸 秀紀*; 伊藤 晋一*; 中島 健次; 河村 聖子

Physica B; Condensed Matter, 562, p.148 - 154, 2019/06


 被引用回数:5 パーセンタイル:50.07(Physics, Condensed Matter)

Seven time-of-flight quasielastic/inelastic neutron scattering instruments are installed on six beamlines in the Materials and Life Science Experimental Facility (MLF) at the Japan Proton Accelerator Research Complex (JPARC). Four of these instruments are chopper-type direct-geometry spectrometers, one is a near-backscattering indirect-geometry spectrometer, and the other two are spin-echo-type spectrometers. This paper reviews the characteristic features, recent scientific outcomes, and progress in development of MLF spectrometers.


A Telescoping view of solute architectures in a complex fluid system

元川 竜平; 小林 徹; 遠藤 仁; Mu, J.*; Williams, C. D.*; Masters, A. J.*; Antonio, M. R.*; Heller, W. T.*; 長尾 道弘*

ACS Central Science, 5(1), p.85 - 96, 2019/01

 被引用回数:28 パーセンタイル:91.57(Chemistry, Multidisciplinary)

We present a hierarchical aggregate model of an organic phase containing a coordination species that acts as a fundamental building unit of higher-order structures formed in the organic phase. We aimed to elucidate the fundamental aspects of the microscopic structure and phase separation occurring in ionic separation and recovery systems during solvent extraction. The coordination species aggregate through a hydrogen-bonding network formed by interaction between the hydrophilic part of the coordination species with extracted water and acid molecules. This reduces the hydrophilic surface area, resulting in subsequent formation of small primal clusters of 2 to 3 nm in diameter. The primal clusters further aggregate due to van der Waals interaction to form large aggregates of $$<$$ 10 nm in diameter. The size of the primal cluster does not depend on the concentration of the coordination species, whereas the size of the large aggregate increases as the aggregation number of the primal clusters increases. We conclude that hybrid interaction is a key driving force in the formation and growth of the hierarchical aggregate and the induction of phase separation of the organic phase.


Materials and Life Science Experimental Facility (MLF) at the Japan Proton Accelerator Research Complex, 2; Neutron scattering instruments

中島 健次; 川北 至信; 伊藤 晋一*; 阿部 淳*; 相澤 一也; 青木 裕之; 遠藤 仁*; 藤田 全基*; 舟越 賢一*; Gong, W.*; et al.

Quantum Beam Science (Internet), 1(3), p.9_1 - 9_59, 2017/12



Inelastic and quasi-elastic neutron scattering spectrometers in J-PARC

瀬戸 秀紀; 伊藤 晋一; 横尾 哲也*; 遠藤 仁*; 中島 健次; 柴田 薫; 梶本 亮一; 河村 聖子; 中村 充孝; 川北 至信; et al.

Biochimica et Biophysica Acta; General Subjects, 1861(1), p.3651 - 3660, 2017/01

 被引用回数:21 パーセンタイル:81.31(Biochemistry & Molecular Biology)



Nanoscopic structural investigation of physically cross-linked nanogels formed from self-associating polymers

関根 由莉奈; 遠藤 仁*; 岩瀬 裕希*; 竹田 茂生*; 向井 貞篤*; 深澤 裕; Littrell, K. C.*; 佐々木 善浩*; 秋吉 一成*

Journal of Physical Chemistry B, 120(46), p.11996 - 12002, 2016/11

 被引用回数:9 パーセンタイル:32.62(Chemistry, Physical)



Small-angle neutron scattering study of specific interaction and coordination structure formed by mono-acetyl-substituted dibenzo-20-crown-6-ether and cesium ions

元川 竜平; 小林 徹; 遠藤 仁*; 池田 隆司; 矢板 毅; 鈴木 伸一; 成田 弘一*; 阿久津 和宏*; Heller, W. T.*

Journal of Nuclear Science and Technology, 53(8), p.1205 - 1211, 2016/08

 被引用回数:0 パーセンタイル:0.01(Nuclear Science & Technology)

This study uses small-angle neutron scattering (SANS) to elucidate the coordination structure of the complex of mono-acetyl substituted dibenzo-20-crown-6-ether (ace-DB20C6) with Cs. SANS profiles obtained for the complex of ace-DB20C6 and Cs (ace-DB20C6/Cs) in deuterated dimethyl sulfoxide indicated that Cs coordination resulted in a more compact structure than the free ace-DB20C6. The data were fit well with SANS profiles calculated using Debye function for scattering on an absolute scattering intensity scale. For this theoretical calculation of the scattering profiles, the coordination structure proposed based on a density functional theory calculation. Consequently, we conclude that the SANS analysis experimentally supports the proposed coordination structure of ace-DB20C6/Cs and suggests the following: (1) the complex of ace-DB20C6 and Cs is formed with an ace-DB20C6/Cs molar ratio of 1/1; (2) the two benzene rings of ace-DB20C6 fold around Cs above the center of the crown ether ring of ace-DB20C6.


Neutron polarization analysis for biphasic solvent extraction systems

元川 竜平; 遠藤 仁*; 長尾 道弘*; Heller, W. T.*

Solvent Extraction and Ion Exchange, 34(5), p.399 - 406, 2016/07

 被引用回数:4 パーセンタイル:21.16(Chemistry, Multidisciplinary)

We performed neutron polarization analysis (NPA) of extracted organic phases containing complexes, comprised of Zr(NO$$_{3}$$)$$_{4}$$ and tri-n-butyl phosphate (TBP), which enabled decomposition of the intensity distribution of small-angle neutron scattering (SANS) into the coherent and incoherent scattering components. The coherent scattering intensity, containing structural information, and the incoherent scattering compete over a wide range of magnitude of scattering vector, $$q$$, specifically when $$q$$ is larger than $$q$$ $$approx$$ 1/$$R_{rm g}$$, where $$R_{rm g}$$ is the radius of gyration of scatterer. Therefore, it is important to determine the incoherent scattering intensity exactly to perform an accurate structural analysis from SANS data when $$R_{rm g}$$ is small, such as the aforementioned extracted coordination species. Although NPA is the best method for evaluating the incoherent scattering component for accurately determining the coherent scattering in SANS, this method is not used frequently in SANS data analysis because it is technically challenging. In this study, we successfully demonstrated that experimental determination of the incoherent scattering using NPA is suitable for sample systems containing a small scatterer with a weak coherent scattering intensity, such as extracted complexes in biphasic solvent extraction system.


Mesoscopic structures of vermiculite and weathered biotite clays in suspension with and without cesium ions

元川 竜平; 遠藤 仁*; 横山 信吾*; 小川 紘樹*; 小林 徹; 鈴木 伸一; 矢板 毅

Langmuir, 30(50), p.15127 - 15134, 2014/12

 被引用回数:21 パーセンタイル:62.87(Chemistry, Multidisciplinary)

The effect of cesium (Cs) adsorption on the mesoscopic structure of the clay minerals vermiculite and weathered biotite (WB) in suspensions was elucidated by small-angle X-ray scattering (SAXS). The clay minerals form multilayered structures and the Cs cations are strongly adsorbed in the interlayer space of the soil clays, in particular vermiculite and WB. SAXS was used to monitor the relationship between Cs adsorption at the clay interlayers and the structural changes at length scales from 0.1 to 100 nm. The variation in the distance between the neighboring clay sheets and the spatial arrangement of the clay sheets with and without Cs were clarified. Our quantitative analyses revealed that the number of stacked layers of pure vermiculite was decreased by Cs addition, whereas that of WB increased. Moreover, the average distance between the neighboring layers of vermiculite in suspension was larger than that of WB, which reflects the different conditions of Cs intercalation. These findings provide fundamental insights that are important for predicting the environmental fate of radioactive cesium in contaminated regions and for developing methods for extracting cesium from soil.


Collective structural changes in vermiculite clay suspensions induced by cesium ions

元川 竜平; 遠藤 仁*; 横山 信吾*; 西辻 祥太郎*; 小林 徹; 鈴木 伸一; 矢板 毅

Scientific Reports (Internet), 4, p.6585_1 - 6585_6, 2014/10

 被引用回数:32 パーセンタイル:76.45(Multidisciplinary Sciences)

Following the Fukushima Daiichi nuclear disaster in 2011, Cs radioisotopes have been dispersed over a wide area. Most of the Cs has remained on the surface of the soil because Cs is strongly adsorbed in the interlayer spaces of soil clays, particularly vermiculite. We have investigated the microscopic structure of an aqueous suspension of vermiculite clay over a wide length scale (0.1-100 nm) by small-angle X-ray scattering. We determined the effect of the adsorption behavior of Cs on the structural changes in the clay. It was found that the abruption of the clay sheets was induced by the localization of Cs at the interlayer. This work provides important information for predicting the environmental fate of radioactive Cs in polluted areas, and for developing methods to extract Cs from the soil and reduce radioactivity.


Dynamics of polystyrene in a theta solvent investigated by neutron spin echo

遠藤 仁

Journal of the Physical Society of Japan, 82(Suppl.A), p.SA014_1 - SA014_6, 2013/01

 被引用回数:2 パーセンタイル:22.18(Physics, Multidisciplinary)

中性子スピンエコー法を用い、$$theta$$溶媒中のポリスチレンのダイナミクスを検証した。最長50ナノ秒までの中間相関関数を観測し、ガウス近似に流体力学的相互作用を考慮したZimm理論と定量的に比較した。その結果、実験結果は散乱ベクトル$$Q$$の小さい領域($$Qtimes b<1$$$$b$$はボンド長)でしかZimm理論と一致せず、$$Q$$の値が大きくなるにつれて徐々に理論から外れていくことが判明した。そのずれは、実験における$$Q$$の最大値(0.1$${rm AA}^{-1}$$)で、減衰係数で比較して約半分であった。


中性子小角散乱; 応用編

遠藤 仁; 杉山 正明*; 井上 倫太郎*

波紋, 22(3), p.258 - 267, 2012/08



Mass production results of superconducting cables for CS and EF coils of JT-60SA

杉本 昌弘*; 小杉 恵三*; 片山 功多*; 伊井 秀樹*; 高木 亮*; 遠藤 壮*; 清水 仁司*; 坪内 宏和*; 木津 要; 吉田 清

Proceedings of 24th International Cryogenic Engineering Conference (ICEC 24) and International Cryogenic Materials Conference 2012 (ICMC 2012) (CD-ROM), p.799 - 802, 2012/05




遠藤 仁

高分子, 60(4), p.193 - 194, 2011/04




遠藤 仁

波紋, 21(1), p.50 - 54, 2011/02



The Static structure of polyrotaxane in solution investigated by contrast variation small-angle neutron scattering

遠藤 仁; 眞弓 皓一*; 大坂 昇*; 伊藤 耕三*; 柴山 充弘*

Polymer Journal, 43(2), p.155 - 163, 2011/02

 被引用回数:6 パーセンタイル:23.16(Polymer Science)



Selective separation of heat-generating nuclide by silica gels loaded with ammonium molybdophosphate; Adv.-ORIENT cycle development

遠藤 祐介*; Wu, Y.*; 三村 均*; 新堀 雄一*; 小山 真一; 大西 貴士; 大林 弘; 山岸 功; 小澤 正基

Proceedings of International Conference on Advanced Nuclear Fuel Cycle; Sustainable Options & Industrial Perspectives (Global 2009) (CD-ROM), p.1007 - 1015, 2009/09

高速炉を機軸とする新しい燃料サイクルの開発を目指した先進オリエントサイクル開発の一環として、発熱元素Csを分離するための複合吸着剤(モリブドリン酸アンモニウム担持シリカゲル,AMP-SG)を複数の方法で調製し、吸着溶離試験を実施した。AMP-SG複合吸着剤は、高レベル廃液相当の2$$sim$$3M HNO$$_{3}$$溶液においても10$$^{3}$$cm$$^{3}$$/g以上の高いCs分配係数を示した。Cs吸着等温線はラングミュア式に従い、この式から求めた最大吸着量は0.24mmol/gであった。アンモニウム塩溶液はCsの回収及び吸着剤再生に有効な溶離剤であり、カラムに吸着したCsの94%を5M NH$$_{4}$$NO$$_{3}$$-1M HNO$$_{3}$$溶液で溶離できた。硝酸-硝酸アンモニウム混合液を用いたクロマトグラフィでは、同族元素であるCsとRbを高純度で分離できることを確認した。



遠藤 祐介*; Wu, Y.*; 三村 均*; 新堀 雄一*; 山岸 功; 小山 真一; 大西 貴士; 小澤 正基

no journal, , 



Measurements of motions of actin by neutron spin-echo spectroscopy

藤原 悟; 松本 富美子; 中川 洋; 遠藤 仁*; 小田 俊郎*

no journal, , 


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